基于TDLAS技术的云水含量检测系统

针对传统云水含量传感器体积大,功耗大等问题,本文基于可调谐半导体激光器吸收光谱技术,研制了一种云水含量检测系统.采用1 368.6nm分布式反馈半导体激光器作为检测光源,设计了基于TLC7528芯片的正交锁相放大器,提高了测量的稳定性和抑制噪声的能力;单板实现了激光器驱动、谐波信号处理、浓度反演功能.系统在不同浓度,不同温度下进行在线检测,实验结果表明,系统响应时间为10s左右,水含量在0~16g/m3范围内误差小于5%,在-55^+60℃条件下可正常工作.该系统体积小,检测精度高,响应速度快,性能不受温度影响,很好地满足了机载云层探测需要.     

染料分子电子激发态振动失相过程的非相干光时延四波混频研究

本文对噁嗪(Oxagine)、甲酚紫(cresyl violet)染料分子的吸收带和吸收边进行了非相干光时延四波混频(TDFWM-IL)的详细研究,得到了有关失相参量的数据,并利用非相干光时延四渡混频的多能理论解释了实验结果和失相参量的物理意义。     

CRYSTAL STRUCTURE DETERMINATION OF 4-ZINC BOVINE INSULIN AT 1.9 (?) RESOLUTION

With the isomorphous difference Fourier method and the restrained least-squares re-finement technique, the crystal structure of 4- zinc bovine insulin in space group R_3 wasdetermined. The final crystallographic residual is 0. 19 at 1. 9A resolution. Based on therefined model, the structural mechanism for prolonged action of 4- zinc insulin is discussed.     

有机物载体Ti/Al(Bu)3/二苯基二甲氧基硅烷催化长链α-烯烃的聚合研究

探讨了3：1和1：1苯乙烯-丙烯酰胺共聚物为载体的Ti系催化剂的合成以及在长链α-烯烃聚合方面的应用．并通过IR、XRD和粘度法手段对有机载体、负载四氯化钛后的结构及长链α-烯烃(C12)聚合物等进行表征．考察了催化剂浓度对聚合结果的影响．     

基于产量理性推测导数的差异产品企业研发决策

文章通过将推测导数引入企业研发的AJ模型，考察差异产品企业在理性或一致性推测的条件下研发策略和研发投入的变化，通过企业产品差异化参数将寡头企业研发决策扩展到产品相关的企业之间，从而扩大了AJ模型均衡的一般性，文章还给出一致性推测条件下的两种不同类别产品企业研发投入最优成本缩减反应曲线斜率和均衡成本缩减量与溢出效应之间的关系。     

用时间分辨简并四波混频研究液晶相变前行为

我们采用时间分辨简并四波混频研究了MBBA液晶相变前分子取向弛豫时间随温度的变化。实验结果与Landau-de Gennes模型的理论预测基本相符。 关键词：     

EXACT RESULTS FOR A SYMMETRIC 27-VERTEX MODEL

Wu study a symmetric 3-state 27-vertex model and summarize three ways con-tributing to obtaining information of a higher-spin (more-vertex) model in terms of lower-spin (less-vertex) models. We find that this model is equivalent to a symmet-ric 2-state 8-vertex model or an arbitrary 3-state spin models on Kagome lattice in different eases. And 21 exact critical lines and a multicritical point (add something that I cannot recognize) are obtained in ten-dimensional weight space.     

Novel One-step Preparation of Functional Ionic Liquids Using Epoxides as Alkylation Reagents

Owing to their unique chemical and physical properties, ionic liquids (ILs) have received focus attention for application as solvent alternatives. ILs can be used in place of organic solvents in synthesis, catalysis, electrochem istry and liquid/liquid extractions. The commonly reported ILs have relied on pyridinium or imidazolium cations bearing simple alkyl groups.     

Na6In4[P7O24(OH)5]·4H2O的水热合成与表征

具有开放骨架结构的金属酸盐在作为微孔材料、非线性光学材料、催化剂载体和离子交换剂等方面具有应用前景 [1] .自从报道第一个具有微孔结构的磷酸铝 [2 ]以来 ,许多其它具有开放骨架结构的金属磷酸盐被合成出来 ,它们的性质和潜在的应用研究也备受关注 [3～ 8] .本文采用温和条件下的水热法 ,合成得到了具有螺旋链状结构的磷酸铟钠盐 [Na6 In4 [P7O2 4 ( OH) 5]· 4H2 O,并采用 X射线单晶衍射方法进行结构测定 ,其结构中包含了共顶角的多面体连接成的螺旋链 ,链间的连接形成多面体四元环和八元环 ,3个四元环围成了一个三配位氧为中心…     

Polyolefin graft copolymers via living polymerization techniques: Preparation of poly(n‐butyl acrylate)‐graft‐polyethylene through the combination of Pd‐mediated living olefin polymerization and atom transfer radical polymerization

Poly(n‐butyl acrylate)‐graft‐branched polyethylene was successfully prepared by the combination of two living polymerization techniques. First, a branched polyethylene macromonomer with a methacrylate‐functionalized end group was prepared by Pd‐mediated living olefin polymerization. The macromonomer was then copolymerized with n‐butyl acrylate by atom transfer radical polymerization. Gel permeation chromatography traces of the graft copolymers showed narrow molecular weight distributions indicative of a controlled reaction. At low macromonomer concentrations corresponding to low viscosities, the reactivity ratios of the macromonomer to n‐butyl acrylate were similar to those for methyl methacrylate to n‐butyl acrylate. However, the increased viscosity of the reaction solution resulting from increased macromonomer concentrations caused a lowering of the apparent reactivity ratio of the macromonomer to n‐butyl acrylate, indicating an incompatibility between nonpolar polyethylene segments and a polar poly(n‐butyl acrylate) backbone. The incompatibility was more pronounced in the solid state, exhibiting cylindrical nanoscale morphology as a result of microphase separation, as observed by atomic force microscopy. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 2736–2749, 2002